| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28822901-28823145 | Common:3; Rare:68 | ||||
| chr16:28824344-28824552 | Common:2; Rare:76 | ||||
| chr16:28843978-28844245 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr16:28844696-28844977 | Rare:93; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:28846216-28846623 | Common:2; Rare:142; Clinvar:7; Clinvar (benign):6 | ||||
| chr16:28863457-28863544 | Rare:17 | ||||
| chr16:28863733-28864001 | Common:3; Rare:65 | ||||
| chr16:28879865-28880048 | Common:3; Rare:55 | ||||
| chr16:28925165-28925408 | Rare:79 | ||||
| chr16:28974642-28974794 | Common:1; Rare:62 | ||||
| chr16:29454014-29454571 | |||||
| chr16:29790576-29790801 | Common:1; Rare:94; Clinvar (benign):2 | ||||
| chr16:29805482-29805707 | Common:2; Rare:106 | ||||
| chr16:29807731-29808196 | Common:2; Rare:235 | ||||
| chr16:29815998-29816751 | Common:2; Rare:253 |